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rs267608073(-;AAG)

From SNPedia
(Redirected from I5037885(D;I))
Variant of uncertain significance; possible Lynch syndrome mutation
Is agenotype
ofrs267608073
GeneMSH6
Chromosome2
Position47,801,023
mentionedby
Magnitude5
ReputeBad
Geno Mag Summary
(-;AAG) 5 Variant of uncertain significance; possible Lynch syndrome mutation
(AAG;AAG) 0 common/normal

Listed in ClinVar as being of uncertain significance, the minor allele of this genotype, causing an in-frame deletion, has been reported in individuals affected with colon, endometrial, and pancreatic cancer, but it has not been proven to be causative.